Cognitive, behavioural and adaptive profiles of children with glutaric aciduria type I detected through newborn screening

Journal of Inherited Metabolic Disease

Volumn 32, Issue SUPPL. 1, 2009, Pages

  Beauchamp, M H ^a,b,c   Boneh, A ^b,c   Anderson, V ^a,b,c  

^a MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

GLUTARYL COENZYME A DEHYDROGENASE;

ADAPTIVE BEHAVIOR; ARTICLE; CASE REPORT; CHILD; CHILD BEHAVIOR; COGNITION; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; HUMAN; MALE; METABOLIC ENCEPHALOPATHY; MOTOR PERFORMANCE; NEUROPSYCHOLOGICAL TEST; NEWBORN; NEWBORN SCREENING; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PSYCHOLOGICAL ASPECT; PSYCHOMOTOR DISORDER; SPEECH SOUND DISORDER;

ADAPTATION, PSYCHOLOGICAL; AMINO ACID METABOLISM, INBORN ERRORS; ARTICULATION DISORDERS; BRAIN DISEASES, METABOLIC; CHILD; CHILD BEHAVIOR; CHILD, PRESCHOOL; COGNITION; GLUTARYL-COA DEHYDROGENASE; HUMANS; INFANT, NEWBORN; MALE; MOTOR SKILLS; MOTOR SKILLS DISORDERS; NEONATAL SCREENING; NEUROPSYCHOLOGICAL TESTS;

EID: 84881075026     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-009-1167-z     Document Type: Article

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